Canonical Allele Identifier: CA467877614

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695367A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800915A>C , CM000671.2:g.137800915A>C	GRCh38
NC_000009.11:g.140695367A>C , CM000671.1:g.140695367A>C	GRCh37
NC_000009.10:g.139815188A>C	NCBI36
NG_011776.1:g.186924A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2643A>C MANE Select	ENSP00000417980.1:p.Thr881=
ENST00000636027.1:c.2529A>C	ENSP00000489961.1:p.Thr843=
ENST00000637161.1:c.2550A>C	ENSP00000490328.1:p.Thr850=
ENST00000637261.1:c.2683A>C	ENSP00000490815.1:n.2683A>C
ENST00000637891.1:c.537A>C	ENSP00000490907.1:p.Thr179=
ENST00000637949.1:c.321A>C	ENSP00000489786.1:p.Thr107=
ENST00000460843.5:c.2643A>C	ENSP00000417980.1:p.Thr881=
ENST00000462942.3:c.1500A>C	ENSP00000436107.1:p.Thr500=
ENST00000482340.5:c.213A>C	ENSP00000486748.1:p.Thr71=
ENST00000486164.5:c.221A>C
ENST00000488242.2:n.169A>C
ENST00000493484.5:c.213A>C	ENSP00000486503.1:p.Thr71=
NM_024757.4:c.2643A>C	NP_079033.4:p.Thr881=
XM_005266105.3:c.2634A>C	XP_005266162.1:p.Thr878=
XM_005266110.1:c.2550A>C	XP_005266167.1:p.Thr850=
XM_006717288.2:c.2625A>C	XP_006717351.1:p.Thr875=
XM_011519021.1:c.2652A>C	XP_011517323.1:p.Thr884=
XM_011519022.1:c.2649A>C	XP_011517324.1:p.Thr883=
XM_011519023.1:c.2631A>C	XP_011517325.1:p.Thr877=
XM_011519024.1:c.2574A>C	XP_011517326.1:p.Thr858=
XM_011519025.1:c.2550A>C	XP_011517327.1:p.Thr850=
XM_011519026.1:c.2508A>C	XP_011517328.1:p.Thr836=
XM_011519027.1:c.2652A>C	XP_011517329.1:p.Thr884=
XM_011519029.1:c.1074A>C	XP_011517331.1:p.Thr358=
XM_011519030.1:c.426A>C	XP_011517332.1:p.Thr142=
XM_011519031.1:c.213A>C	XP_011517333.1:p.Thr71=
XM_011519032.1:c.213A>C	XP_011517334.1:p.Thr71=
XM_011519033.1:c.2487A>C	XP_011517335.1:p.Thr829=
NM_001354263.1:c.2622A>C	NP_001341192.1:p.Thr874=
XM_005266105.5:c.2634A>C	XP_005266162.1:p.Thr878=
XM_011519021.3:c.2652A>C	XP_011517323.1:p.Thr884=
XM_011519022.3:c.2649A>C	XP_011517324.1:p.Thr883=
XM_011519023.3:c.2631A>C	XP_011517325.1:p.Thr877=
XM_011519029.3:c.1074A>C	XP_011517331.1:p.Thr358=
XM_011519030.3:c.426A>C	XP_011517332.1:p.Thr142=
XM_017015134.1:c.2628A>C	XP_016870623.1:p.Thr876=
XM_017015136.2:c.2544A>C	XP_016870625.1:p.Thr848=
XM_017015137.1:c.2529A>C	XP_016870626.1:p.Thr843=
XM_017015138.1:c.2529A>C	XP_016870627.1:p.Thr843=
XM_024447674.1:c.2472A>C	XP_024303442.1:p.Thr824=
XM_024447675.1:c.2406A>C	XP_024303443.1:p.Thr802=
XM_024447676.1:c.1767A>C	XP_024303444.1:p.Thr589=
XM_024447677.1:c.1767A>C	XP_024303445.1:p.Thr589=
XM_024447678.1:c.2550A>C	XP_024303446.1:p.Thr850=
XM_024447680.1:c.2385A>C	XP_024303448.1:p.Thr795=
NM_024757.5:c.2643A>C MANE Select	NP_079033.4:p.Thr881=
NM_001354263.2:c.2622A>C	NP_001341192.1:p.Thr874=